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Symptom orientation: Autism - A collection of scientific studies & other sources!

CONTENT
  1. Symptom orientation!
  2. Autism!
  3. Aluminium damages Neurons!
  4. mRNA vaccines cause autism
  5. Connected articles

1. Symptom orientation!

General view on distraction from solutions by declaring the symptoms of the diseases to be their reasons.
https://geoarchitektur.blogspot.com/p/symptom-orientation-autism-cancer.html

Chapters of this article have been put into separate pages.


2. Autism!

Vaccines are propagated to protect us by controlled immunization against various pathogens. Since the invention of vaccination the amount of vaccines has grown and the materials have been modified. The idea of vaccinating children to give harden their immune system at the start of their life may sound good, but what if the correlation indicates that at least some vaccines are more damaging than helping?



Or take this one! Why is the autism rate now about 1 of 50?


Should we ignore this correlation?

Should the pharma corporations ignore it, because else they would damage their revenues?

Should the governments ignore it, to protect the economy and workforce of the pharma industry?

Should the employees of pharma corporations accept having autistic children as a collateral damage of having income?

Should the medics and scientists observing this correlation prevent researching the reasons?

There are some studies which don't support the assumption of MMR (measles, mumps and rubella) vaccines would cause autism, but they don't deliver the explanation for the correlation or another reason of autism either!

Vaccines and Autism: A Tale of Shifting Hypotheses
Stanley Plotkin Jeffrey S. Gerber Paul A. Offit
Clinical Infectious Diseases, Volume 48, Issue 4, 15 February 2009, Pages 456–461,
https://doi.org/10.1086/596476 Published:15 February 2009
https://academic.oup.com/cid/article/48/4/456/284219/Vaccines-and-Autism-A-Tale-of-Shifting-Hypotheses

"Twenty epidemiologic studies have shown that neither thimerosal nor MMR vaccine causes autism. These studies have been performed in several countries by many different investigators who have employed a multitude of epidemiologic and statistical methods. The large size of the studied populations has afforded a level of statistical power sufficient to detect even rare associations. These studies, in concert with the biological implausibility that vaccines overwhelm a child's immune system, have effectively dismissed the notion that vaccines cause autism. Further studies on the cause or causes of autism should focus on more-promising leads."

They invest huge efforts to protect the MMR and thimerosal markets, but don't spend a cent in researching the causes of autism! Can we trust such guys, because they name their marketing papers "studies"?

If they don't know the real reason yet, why don't they stop using MMR and thimerosal for vaccination to go back to the former methods and materials and empirically rule out any involvement of MMR and thimerosal in the rise of autism?

There is only one answer to that question!
They protect the investments in MMR and thimerosal!
 
They don't protect the health of the children!
They don't care about health, they only care for the business!

This conclusion alone should prevent any direct or indirect involvement of pharma corporations in research and development of medicine, particularly vaccines.

The best way of business protection is to blame the victims for their devastation!

What causes autism?
https://www.autismspeaks.org/what-autism/learn-more-autism/what-causes-autism

Whenever a collateral disease with epidemic scale has to be hidden from minds, the answers are always the same! They are made to blame the victims!

"
  • Autism’s genetic risk factors
  • Autism’s environmental risk factors
  • Advanced parent age (either parent)
  • Pregnancy and birth complications (e.g. extreme prematurity [before 26 weeks], low birth weight, multiple pregnancies [twin, triplet, etc.])
  • Pregnancies spaced less than one year apart
  • Differences in brain biology
"

Genetics, environment, parental age, pregnancy complications, different biology and all the other aspects existed also before the use of MMR and thimerosal! Why should all that be blamed?

But it is never what empirically correlates!

"No effect on risk:

Vaccines. Each family has a unique experience with an autism diagnosis, and for some it corresponds with the timing of their child’s vaccinations. At the same time, scientists have conducted extensive research over the last two decades to determine whether there is any link between childhood vaccinations and autism. The results of this research is clear: Vaccines do not cause autism. The American Academy of Pediatrics has compiled a comprehensive list of this research. You can view and download the list here."

These "studies" are not scientific evidence. They don't research the reaction of the vaccine materials in the body and verify or falsify the impact. They only play with statistics! Following a academic form doesn't make them scientific. Making the publication look scientific is the best working form of deceit. The notion "scientific" is abused like a religious dogma. You are expected to "believe in science" and accept and not resist the fraud!

Vaccines Cause Autism
http://www.healingourchildren.net/Vaccine/vaccines_cause_autism.htm

"Firstly, vaccines contain both mercury and aluminum. See the Centers for Disease Control (CDC) additives chart."

"During the supposed 1999-2002 phase out mercury in vaccines. The Centers for disease control suggested that pregnant women in their first trimester receive a dosage of mercury labeled as a "flu vaccine." (CDC MMWR 205;54 (41):1050-52)"

"After the phase out, aluminum content was increased in vaccines in HEP A. Babies who follow the CDC immunization schedule recieve 5mg (5000 mcg) of aluminum by 18 months of age."

"When Mercury is Removed from the Body - Autism symptoms leave."

DID YOU KNOW? 1 IN 6 CHILDREN NOW HAS A DEVELOPMENTAL DISABILITY IN THE U.S.
Truth Frequency Radio, Aug 26, 2014, Melissa Melton
http://tfrlive.com/did-you-know-1-in-6-children-now-has-a-developmental-disability-in-the-u-s/

"The rates of autism have skyrocketed and continue to get worse each year in this country. The CDC now estimates autism effects 1 in 68 children in the U.S., up a whopping 30% from 2012. For boys, the rate is now 1 in 42. The CDC continues to say genes play a role, but the agency readily admits it doesn’t know what is causing all this autism."

"The prevalence rate for autism before 1990 was only three children per 10,000. When the CDC began surveillance of the study population in 2000, it was one child in every 150. Look at the chart above. Autism just keeps going up."

"Back in 2009, when the autism rates first rocketed to 1 in 88, the Environmental Working Group suggested exposure to neurotoxic chemicals could definitely play a role: most notably, mercury."

All big crimes seem to begin with an "Act"!

"The federal Toxic Substances Control Act has allowed the chemical industry to flood the marketplace with toxic chemicals, including neurotoxins, with virtually no proof they are safe for people."

"Then again, the CDC is currently ignoring a whistleblower within its own ranks who came forward to admit that the agency knowingly manipulated data to hide a link in one of its major studies between the MMR vaccine and autism — a link which showed a 340% increase in autism specifically in African American boys given an MMR shot at age three or younger."

"Even if you pretend that isn’t happening, America has the most aggressive mandated vaccine schedule in the world. The CDC now recommends up to 37 shots of 14 different vaccinations by the age of two, prompting the National Vaccine Information Center to ask, “Is the atypical manipulation of the immune system with more and more vaccines in early life setting some children up for chronic disease and disability?”"

"Why not? The pediatric and adolescent vaccine market is set to be worth over $16 billion by 2016, and no one pushes those shots harder than the CDC, a well-known revolving door with Big Pharma."

"It isn’t hard to see where the mutually beneficial arrangement between CDC and Big Pharma would keep the agency pointing its finger at anything other than the products its pushing."

"Our children are being damaged en masse in this country, but none of these so-called medical experts running the show can seem to figure out why? The alarming rise in autism and developmental disabilities in this country are just such a great “mystery,” right?"

Autism risk 420% higher in vaccinated children vs. non-vaccinated, published science confirms
Thursday, June 01, 2017 by: Vicki Batts
https://www.naturalnews.com/2017-06-01-autism-risk-420-higher-in-vaccinated-children-vs-non-vaccinated-published-science-confirms.html

"A recent study led by researchers from the School of Public Health at Jackson State University has come to some shocking conclusions about vaccinated children. Perhaps one of the most jaw-dropping finds was that vaccinated children exhibited a 420 percent higher incidence of autism when compared to non-vaccinated children — as well as a staggering increased incidence of neurodevelopmental disorders (NDD) in general."

Übersicht Autismus und Vitamin D
https://www.vitamindwiki.com/Overview+Autism+and+vitamin+D

VAXXED from Cover-up to Catastrophe
https://vaxxedthemovie.com/

"In 2013, biologist Dr. Brian Hooker received a call from a Senior Scientist at the U.S. Centers for Disease Control and Prevention (CDC) who led the agency’s 2004 study on the Measles-Mumps-Rubella (MMR) vaccine and its link to autism.

The scientist, Dr. William Thompson, confessed that the CDC had omitted crucial data in their final report that revealed a causal relationship between the MMR vaccine and autism. Over several months, Dr. Hooker records the phone calls made to him by Dr. Thompson who provides the confidential data destroyed by his colleagues at the CDC.

Dr. Hooker enlists the help of Dr. Andrew Wakefield, the British gastroenterologist falsely accused of starting the anti-vax movement when he first reported in 1998 that the MMR vaccine may cause autism. In his ongoing effort to advocate for children’s health, Wakefield directs this documentary examining the evidence behind an appalling cover-up committed by the government agency charged with protecting the health of American citizens.

Interviews with pharmaceutical insiders, doctors, politicians, and parents of vaccine-injured children reveal an alarming deception that has contributed to the skyrocketing increase of autism and potentially the most catastrophic epidemic of our lifetime."

Robert DeNiro: "Everyone Should See Vaxxed"
Apr 15, 2016



4. Aluminium damages Neurons!

Here is a copy of summarizing articles with further references, which extensively explain the various evidence about the cell damaging effects of Aluminium. Knowing all that, how anyone with conscience inject this poison into the body of small children, where it crosses the blood-brain barrier and destroys the central nerval system. The brains of the children destroyed forever by a single vaccine!

More of such scientific evidence can be found, but every parent having a child with autism is well aware the moment of brain damage after a vaccine injections. No one needs to study biology and medicine and write extensive papers to be aware of this crime, but as people believe in "science" more than they believe in God, it is necessary to show them that the brain damage by Aluminium injections is scientifically evident.

Autism is the result of damaging and killing neuronal cells by Aluminium, Mercury and other poisonous content of injections under the pretext of vaccinations!
  • Aluminium induced Various adverse effects on the mammalian Central nervous system (CNS = brain)
  • Amyotrophic Lateral Sclerosis (ALS), 
  • Alzheimer’s disease (AD), dementia, 
  • Gulf war syndrome
  •  Parkinsonism
  • Aluminium-induced oxidative stress
  • Aluminium as a cholinotoxic agent
  • Al affect gene expression by altering the expression of cerebral proteases
  • Aluminium induced activatation of monoamine oxidase isotypes in brain.
  • Aluminium binds to the histone-DNA complex
  • Alumininium induces conformational changes
  • Aluminium nduces topological changes of DNA
  • Effect of aluminium on cell mediated excitotoxicity
  • Effect of aluminium on calcium homeostasis
  • Aluminium induced apoptosis
  • Aluminium induced inflammatory responses in the brain
  • Aluminium induced neurofibrillary tangles (NFTs)
  • increase in prostaglandin E2
Multifaceted effects of aluminium in neurodegenerative diseases: A review
Author links open overlay panelS. Maya, T. Prakash, Krishna Das Madhu, Divakar Goli

"Abstract

Aluminium (Al) is the most common metal and widely distributed in our environment. Al was first isolated as an element in 1827, and its use began only after 1886. Al is widely used for industrial applications and consumer products. Apart from these it is also used in cooking utensils and in pharmacological agents, including antacids and antiperspirants from which the element usually enters into the human body. Evidence for the neurotoxicity of Al is described in various studies, but still the exact mechanism of Al toxicity is not known. However, the evidence suggests that the Al can potentiate oxidative stress and inflammatory events and finally leads to cell death.

Al is considered as a well-established neurotoxin and have a link between the exposure and development of neurodegenerative diseases, including Amyotrophic Lateral Sclerosis (ALS), Alzheimer’s disease (AD), dementia, Gulf war syndrome and Parkinsonism. Here, we review the detailed possible pathogenesis of Al neurotoxicity. This review summarizes Al induced events likewise oxidative stress, cell mediated toxicity, apoptosis, inflammatory events in the brain, glutamate toxicity, effects on calcium homeostasis, gene expression and Al induced Neurofibrillary tangle (NFT) formation. Apart from these we also discussed animal models that are commonly used for Al induced neurotoxicity and neurodegeneration studies. These models help to find out a better way to treat and prevent the progression in Al induced neurodegenerative diseases."

"Introduction

Al, the third most abundant element and the most common metal in the earth's crust and it is ubiquitous in the environment. Al toxicity only happens when exposure to an extremely high level of Al content and it is unavoidable. Al enters into the human body through drinking water, food, use of utensils, deodorants, and drugs [1]. It is estimated that the dietary intake of Al can be from 3 to 30 mg/day [2]. Most of the Al compounds are relatively insoluble at physiological pH, limiting absorption of Al through ingestion or inhalation (only 0.06% to 0.1% absorbed). Al toxicity results due to an exposure to large amounts of Al containing compounds or direct inoculation of Al via dialysates, parenteral nutrition, or implanted foreign materials, such as surgical cements. In the brain Al accumulates in the sensitive area such as hippocampus and frontal cortex and is considered as a contributing factor in the pathogenesis of neurodegenerative diseases [1].

Normally Al has no known physiological role. The toxic consequences of Al exposure are thought to be related to dysregulation of other essential metals or ions; deposition of insoluble Al precipitates in vulnerable tissues; or proteins, lipids, or nucleotic interactions resulting in conformational and structural alterations, aggregation, and functional alterations. Neurological consequences of toxic Al exposure include Encephalopathy, Seizures, Motor neuron degeneration, Parkinsonism and death. Al mediated neurodegeneration resulting in cognitive dysfunction has been associated with elevated amyloid precursor protein (APP) expression [3], [4], amyloid β (Aβ) deposition [5], [6], impaired cholinergic projections and apoptotic neuronal death [7], [8], [9].

Al toxicity generally caused by the disruption of homeostasis of metals such as magnesium, calcium, and iron: in fact, Al mimics these metals in their biological functions and triggers many biochemical alterations [10]. Al exerts direct genotoxicity in primary human neuronal cells and induces neurodegeneration, through an increase in iron accumulation and oxygen reactive species (ROS) production [11]. Al induces neurotoxicity primarily by triggering oxidative stress that affects a large number of signaling cascades and ultimately causes cellular death. Al induced oxidative damage to DNA has been previously associated with neurodegeneration in different regions of the rat brain [12]. Most of the studies suggests that the removal of toxic metal from human body can represent a useful tool to avoid the beginning or progression of many diseases related to metal intoxication [13]."

"Section snippets

Aluminium-induced oxidative stress

Al chloride accelerates iron mediated lipid peroxidation (LPO) and the results marked oxidative damage by increasing the redox active iron concentration in the brain. Increased Oxy-radicals and loss of cellular homeostasis cause oxidative stress that leads to neurotoxicity [14]. The oxidative products released in the neurons are malondialdehyde, carbonyls, peroxynitriles, nitrotyrosines, and enzymes like super oxide dismutase (SOD), haemoxygenase-I, etc. [15]. The imbalance in oxidative

Aluminium as a cholinotoxic agent

Cholinergic functions of the central nervous system (CNS) mainly depend on the neurotransmitter acetylcholine (ACh). After release from presynaptic nerve terminals, ACh is rapidly removed from the synaptic cleft by Acetylcholine esterase (AChE), which belongs to the family of type B carboxyl esterases and cleaves ACh into inactive metabolites, choline and acetate [22]. As cholinotoxic, Al chloride produces functional change in the cholinergic and noradrenergic neurotransmission. 

AChE is Aluminium induced neurotoxicity

Al is reported to influence a number of important reaction and it results various adverse effects on the mammalian Central nervous system (CNS). It includes important reactions for brain development such as the axonal transport, neurotransmitter synthesis, synaptic transmission phosphorylation or dephosphorylation of proteins, protein degradation, gene expression, and inflammatory responses.

Al exhibits in only one oxidation, Al3+. It has a greater affinity towards negatively charged,
Aluminium on gene expression

Al affect gene expression by altering the expression of cerebral proteases and by activating monoamine oxidase isotypes in brain [24]. Al binds to the histone-DNA complex and induces conformational changes and also induces topological changes of DNA [25], [26], [27]. The studies show that there is an elevated level of glial cell marker TNF-α and glial fibrillary acidic protein (GFAP) [28]. Also Al induces the expression of NF-κB subunits, interleukin-1β precursor, phospholipase A2 and DAXX that

Effect of aluminium on cell mediated excitotoxicity

Al causes the mitochondrial damage leading to the generation of highly reactive oxy and hydroxyl free radicals and cause accumulation of hydrogen peroxide. The increased hydrogen peroxide pool enhances the presence of redox active iron either from loosely bound iron or by modulating the electron transport chain [38]. Also Al enhances oxidative stress through enhanced iron-mediated Fenton reactions by increasing the redox active iron concentrations. Studies shows that Al activates superoxide

Effect of aluminium on calcium homeostasis

Al also induce neuronal injury by interfering calcium homeostasis. Al delay the closure of voltage-dependent calcium channels and block calmodulin (CaM)-dependent Ca2+/Mg2+-ATPase, which is responsible for the protective mechanism against excitotoxicity [42]. The studies also show that, there is an increase in glutamate levels while their γ-aminobutyric acid (GABA) brain levels were decreased, a condition that maximizes excitotoxic damage in rats [43]."

"Al rise to metabolic changes likewise,

Aluminium induced apoptosis

Al induces cytochrome c release from mitochondria, a decrease in Bcl-2 in both mitochondria and endoplasmic reticulum, Bax translocation into mitochondria, activation of caspase-3, and DNA fragmentation [8]. The released cytochrome c from mitochondria binds to Apaf-1 and initiates Al induced apoptosis cascade [45]. The formed complex activates caspase-9, that in turn activates the effector caspase that is caspase-3. The released cytochrome c involved in three distinct pathways like, opening of 

Aluminium induced inflammatory responses in the brain

Most of the observations from the studies demonstrate aluminium induced inflammatory responses. Involvement of lipoxygenase and cyclooxygenase-mediated arachidonic acid turnover has been suggested in the Al-induced platelet activation [49]. Al was found to elevate the proinflammatory cytokines, TNF-α, and IL-1α. When the brain cells getting injured, the intracellular Ca2+ rises and also produce reactive oxygen species. While potentially damaging via their direct actions, Ca2+ and free radicals 

Aluminium induced neurofibrillary tangles (NFTs)

NFTs are the aggregates of phosphorylated tau protein and found as a marker for neurodegenerative diseases, namely Alzheimer’s disease (AD) and ALS. The studies show that Aluminium can induce abnormality in cytoskeletal protein such as neurofilaments and/or tau, and causes the formation of NFT and neurodegeneration of motor neurons in ALS [52]. Tau is bound by microtubules in healthy neurons, and is essential to form and function of the neuronal cytoskeleton. Al-ATP, like glutamate, stimulates

Other aluminium induced changes in the brain

Some studies show that there is an increase in prostaglandin E2 (PGE2), prostaglandin A1 (PGA1), and thromboxane A2 (TXA2) in rat hippocampus [62]. The exact mechanism behind the prostaglandin induced neurodegeneration is still unknown. But the studies show that apart from prostaglandin, thromboxane, and cytokine receptors, toll-like receptors (TLRs), on both glia and neurons that likely mediate the neuroinflammatory responses. PGE2, one of the product of inflammatory reactions, and PGA1, which 

Animal models for aluminium toxicity

Although Al3+ exposures have been associated with the development of the most common neurodegenerative disorders, the molecular mechanisms behind the Al3+ transport in neurons and subsequent neuron damage has remained elusive [68]. This review describes some animal models for Al induced neurotoxicity or neurodegeneration

Summary

Although there is lots of evidence that implicates Al in the progression of events that leads to neurodegenerative diseases, some of the evidence remains controversial. However, it is widely accepted that Al is a recognized neurotoxin and that could cause neurodegeneration. Al is a highly abundant and ubiquitously distributed as environmental and industrial toxicant and is also contained in many food products, being involved in skeletal, hematological, and neurological diseases. Once Al reached"


Reading the quotations of the next article, please be aware!
  • "Exposure to Al from only few vaccines can lead to cognitive impairment and autoimmunity in adults"
  • "Is it unreasonable to question whether the current pediatric schedules, often containing 18 Al adjuvanted vaccines, are safe for children?"
  • "significant correlation exists between the amounts of Al administered to preschool children and the current prevalence of ASD in seven Western countries, particularly at 3–4 months of age"
  • "It remains surprising that in spite of over 80 years of use, the safety of Al adjuvants appears to rest largely on assumptions rather than experimental evidence."
  • "Nothing is known about the toxicology and pharmacokinetics of Al compounds in infants and children."
  • "The mechanisms by which Al adjuvants interact with the immune system remain far from clear."
  • "It is notable that many vaccine trials usually use an Al adjuvant containing “placebo” or another vaccine as the “control” group."

Do aluminum vaccine adjuvants contribute to the rising prevalence of autism?
Author links open overlay panelLucija Tomljenovic a, Christopher A. Shaw a bShow more
https://doi.org/10.1016/j.jinorgbio.2011.08.008Get rights and content

"Abstract

Autism spectrum disorders (ASD) are serious multisystem developmental disorders and an urgent global public health concern. Dysfunctional immunity and impaired brain function are core deficits in ASD. Aluminum (Al), the most commonly used vaccine adjuvant, is a demonstrated neurotoxin and a strong immune stimulator. Hence, adjuvant Al has the potential to induce neuroimmune disorders.

When assessing adjuvant toxicity in children, two key points ought to be considered: 

(i) children should not be viewed as “small adults” as their unique physiology makes them much more vulnerable to toxic insults; and 

(ii) if exposure to Al from only few vaccines can lead to cognitive impairment and autoimmunity in adults, is it unreasonable to question whether the current pediatric schedules, often containing 18 Al adjuvanted vaccines, are safe for children? 

By applying Hill's criteria for establishing causality between exposure and outcome we investigated whether exposure to Al from vaccines could be contributing to the rise in ASD prevalence in the Western world. 

Our results show that: 

(i) children from countries with the highest ASD prevalence appear to have the highest exposure to Al from vaccines; 

(ii) the increase in exposure to Al adjuvants significantly correlates with the increase in ASD prevalence in the United States observed over the last two decades (Pearson r = 0.92, p < 0.0001); and 

(iii) a significant correlation exists between the amounts of Al administered to preschool children and the current prevalence of ASD in seven Western countries, particularly at 3–4 months of age (Pearson r = 0.89–0.94, p = 0.0018–0.0248). 

The application of the Hill's criteria to these data indicates that the correlation between Al in vaccines and ASD may be causal. Because children represent a fraction of the population most at risk for complications following exposure to Al, a more rigorous evaluation of Al adjuvant safety seems warranted."

"Introduction

During prenatal and early postnatal development the brain is extremely vulnerable to neurotoxic insults [1], [2]. Not only are these highly sensitive periods of rapid brain development in general [3] but also, the blood brain barrier (BBB) is incomplete and thus more permeable to toxic substances during this time [2], [4], [5]. Further, immune challenges during early development, including those induced by vaccines, can lead to permanent detrimental alterations of nervous and immune system function [6], [7], [8], [9]. Experimental evidence also shows that simultaneous administration of as little as two to three immune adjuvants, or repeated stimulation of the immune system by the same antigen, can overcome genetic resistance to autoimmunity in animals [10], [11]. Moreover, in adult humans, a variety of conditions encompassed by the ‘Autoimmune/inflammatory syndrome induced by adjuvants’ (‘ASIA’) have been linked to exposure to aluminum (Al) vaccine adjuvants (Table 1).

In many Western countries, by the time children are 4–6 years old they will have received a total of 23–32 vaccines [12], [13], many with Al adjuvants, through routine pediatric vaccine schedules [2], [14]. According to the United States Food and Drug Administration (US FDA), safety assessments for vaccines have often not included appropriate toxicity studies because vaccines have not been viewed as inherently toxic [15]. However, if a few vaccines administered to adults can result in adverse outcomes, such as the ‘ASIA’ syndrome, should we assume without experimental evidence that the current pediatric schedules are safe for children?

Analysis of the relevant data shows that the number of vaccinations recommended prior to school entry increased from 10 in the late 1970s to 32 in 2010 (18 of which contain Al adjuvants) [16]. During this same period, the prevalence of autism spectrum disorders (ASD) in the US also increased by as much as 2000% [16]. While such observations have been of interest, the potential role of vaccines in the development of ASD remains controversial. ASD are characterized by marked impairments in social skills, verbal communication, behavior and cognitive dysfunction [17], [18], [19]. Although the etiology of 90% of ASD is still largely unknown [20], [21], a growing body of scientific literature shows that neuroimmune abnormalities (i.e., abnormal cytokine profiles, neuroinflammation and presence of autoantibodies against brain proteins) occur in ASD patients and may contribute to the diversity of ASD phenotypes [17], [20], [22], [23], [24], [25], [26].

Al is an experimentally demonstrated neurotoxin whose ability to impact the human nervous system has been known for decades [16], [27], [28], [29]. For example, exposure to as little as 20 μg/kg bw of Al for period > 10 days is sufficient to cause neurodevelopmental delays in preterm infants [28]. In addition, Al is a potent stimulator of the immune system, indeed this is the very reason why it is used as an adjuvant [14], [30], [31], [32], [33], [34]. Given this, it remains surprising that in spite of over 80 years of use, the safety of Al adjuvants appears to rest largely on assumptions rather than experimental evidence. For example, nothing is known about the toxicology and pharmacokinetics of Al compounds in infants and children [35]. In addition, the mechanisms by which Al adjuvants interact with the immune system remain far from clear [34], [35]. In this regard it is notable that many vaccine trials usually use an Al adjuvant containing “placebo” or another vaccine as the “control” group [36], [37], [38], rather than a saline control. This study design has not allowed a direct comparison of the efficacy and safety of the antigen alone versus the Al adjuvant. In spite of these gaps in our knowledge about Al adjuvants, the use of Al in vaccines is widely regarded as safe and effective [35], [39], [40].

Should it be of concern that so little is known about the potential deleterious impacts of Al adjuvants on the developing central nervous system (CNS) given that worldwide, preschool children are regularly exposed to significant amounts of Al from vaccines [2], [14]? To address this question, we investigated pediatric vaccine schedules from various Western countries in order to gain a better understanding of potential Al exposure from vaccines in children. Our results, supported by the Hill's criteria for establishing causality between exposure and outcome [41], suggest that a causal relationship may exist between the amount of Al administered to preschool children at various ages through vaccination and the rising prevalence of ASD."


4. mRNA vaccines cause autism!





4. Connected articles

Symptom orientation: Cancer - A collection of scientific studies!

Symptom orientation: Fibromyalgia - A collection of scientific studies!

Symptom orientation: Psoriasis - A collection of scientific studies!
https://geoarchitektur.blogspot.com/p/symptom-orientation-psoriasis.html

Symptom orientation: Multiple Sclerosis - A collection of scientific studies!
https://geoarchitektur.blogspot.com/p/symptom-orientation-multiple-sclerosis.html

Symptom orientation: More about VitaminD - A collection of scientific sources!
https://geoarchitektur.blogspot.com/p/symptom-orientation-more-about-vitamind.html

HEALTHY LIGHT!

VitaminD deficiency & SRM chemtrails! #MIH tooth disease!

Burka prevents VitaminD & destroys the society!


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Attention! The visitor of the blog could fall away from his supposed knowledge and beliefs! Read and watch at your own responsibility! Achtung! Der Besucher des Blogs könnte von seinen vermeintlichen Kenntnissen und Überzeugungen abfallen! Lesen und Anschauen auf eigene Verantwortung!
Replace CLIMATE CHANGE by CLIMATE CONTROL to decode all manipulation about that easily! Ersetze KLIMAWANDEL durch KLIMAKONTROLLE, um alle Manipulationen darüber leicht zu entschlüsseln!

QUESTION YOUR KNOWLEDGE, CLOSE YOUR GAPS !!

I am suspended on twitter and blocked on fakebook! So don't miss me there.
Also admins of some Diaspora pods are limiting my activity against ClimateControl. Most are not employed to act as censors, they are MindControlled by NLP.

You feel Your chains when You move!
ClimateControl Mafia is desperate!

Evidence of Water Delivery by ClimateControl!

Water Delivery by ClimateControl Irkaya Farm- Qatar

PROPAGANDA FRAME

Klimakontrol-Lobby hat mit Daniele Ganser und Co. KenFM geentert!
Klimakontrolle ist die Ursache des Klimawandels, nicht dessen Lösung!
Bitte achtet! An dem, was sie verschweigt, sollte die Falsche-Alternative erkannt werden!

MAN MADE CLIMATE BY GEOENGINEERING

GEOENGINEERING is changing weather and climate to grab TROPOSPHERIC WATER by SRM and HAARP for FRACKING and FARMING in DESERTs!

Geoengineering is never the solution against but the reason of killing and devastating changes!

This blog is absolutely not "peer reviewed" and not written by a "renown" scientiputa!
You can verify all content by Yourself!
Evidence and knowledge is not hidden from eyes, but only from minds! Just open Your mind!

BE SITTING WHEN YOU WAKE UP!
BEING DUMBIFIED IS NOT AN APOLOGY FOR BEING DUMBIFIED!
It is NUCLEAR FRACTURING, not hydraulic!
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Lizenz von Enkidu Gilgamesh - Sharing is Caring!

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